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Minnesota Healthy Brain Initiative

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02881788
Enrollment
690
Registered
2016-08-29
Start date
2016-08-01
Completion date
2018-06-01
Last updated
2020-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Ability, General

Brief summary

Minnesota Healthy Brain Initiative will be an ongoing project that aims to increase awareness regarding brain health and its maintenance as well as increasing awareness of the impact of alcohol on brain function. In the immediate future, we hope to obtain data from a non-injured normative, diverse population represented by the state fair patrons.

Detailed description

We hypothesize that a non-invasive 30-minute test, requiring a subject to complete questionnaires and watch images on a TV screen, will yield information relevant to both diagnosis and prognosis of neurological state. To clarify, these tests will not produce information that would involve a diagnostic finding for the participants. We will measure eye movements under a range of visual conditions, including saccades, fixations, smooth pursuit, scan paths and optico-kinetic nystagmus After receiving proper introduction and signing the proper consent forms, the subject will receive instructions to carry out cognitive assessments and answer verbal questionnaires. The subject will also undergo eye tracking. In order to validate the data collected by our eye-trackers, we may ask the subject to complete a non-invasive vision assessment and a breathalyzer assessment. Due to the nature of the breathalyzer assessment, we have decided not to administer the breathalyzer assessment to subjects who are under the age of 21 and/or pregnant. We also refuse to disclose the results of the breathalyzer assessment to the subject since the data will be collected only for research purposes. Subjects' eye movements will be tracked binocularly at a fixed distance from a computer monitor over a brief time period. The visual stimuli will be video clips appropriate for a general or pediatric audience. If at any point the subject becomes uncomfortable, the procedure will be aborted and can be resumed at a later time.

Interventions

None listed

Sponsors

Hennepin County Medical Center, Minneapolis
CollaboratorOTHER
Hennepin Healthcare Research Institute
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
4 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

Males and Females Ages 4-100 All racial and ethnic origins will have an opportunity to participate

Exclusion criteria

Blind in one or both eyes Unable to open eyes Unable to detect light in either eye

Design outcomes

Primary

MeasureTime frameDescription
Eyetracking0-1 yrThe subject will complete a non-invasive eye tracking assessment. Our camera will follow the movement of their eye to assess the patterns made.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026